Starch granule characterization by kinetic analysis of their stages during enzymic hydrolysis: 1H nuclear magnetic resonance studies

被引:16
作者
Dona, Anthony C. [1 ,2 ]
Pages, Guilhem [1 ]
Gilbert, Robert G. [2 ]
Kuchel, Philip W. [1 ]
机构
[1] Univ Sydney, Sch Mol Biosci, Sydney, NSW 2006, Australia
[2] Univ Queensland, Ctr Nutr & Food Sci, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
alpha-Amylase (EC 3.2.1.1); Glucoamylase (EC 3.2.1.3); Digestion kinetics; Product inhibition; Rapidly digested starch; Slowly digested starch; Michaelis-Menten kinetics; Time-resolved nuclear magnetic resonance; spectroscopy; NMR; GLYCEMIC INDEX; ALPHA-AMYLASE; IN-VITRO; RESISTANT STARCH; RICE STARCH; N-ACETYLCYSTEINE; POTATO STARCHES; CHAIN-LENGTH; WHEAT-STARCH; DIGESTION;
D O I
10.1016/j.carbpol.2010.10.042
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
H-1 nuclear magnetic resonance (NMR) spectroscopy was used to study the kinetics of digestion of starch enzymes: specifically we studied the reactions of a-amylase from B. licheniformis (E.C. 3.2.1.1) and glucoamylase from Aspergillus niger (E.C. 3.2.1.3) with starch granules (early stages of digestion) and with oligosaccharides (a later stage). This was done to provide a characterization of starch granules from various sources, with respect to the kinetics of glucose release from them. For the smaller oligosaccharides, a-amylase was inhibited by its reaction product maltose, while glucoamylase was not inhibited by its main product, glucose. The hydrolysis of oligosaccharides up to seven glucose units in length (maltoheptaose) followed Michaelis-Menten kinetics. For starch granules, experimental evidence suggests that the digestion kinetics changes subsequent to the hydrolysis of starch chains, which are accessible to enzymic attack. The rapid-digestion stage, consisting of enzymic attack on accessible starch chains, was precisely described by classical Michaelis-Menten kinetics, without considering product inhibition. During the slow-digestion stage, the rate decreased significantly: this is posited as being due to the inaccessibility of inter-glucose linkages becoming the rate-determining step. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1775 / 1786
页数:12
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